Evidence map›Paper›PMID 30656477›Full record

ArticleEuropean journal of nutrition2020

Genotypes of HLA, TCF7L2, and FTO as potential modifiers of the association between sweetened beverage consumption and risk of LADA and type 2 diabetes.

Josefin E Löfvenborg, Emma Ahlqvist, Lars Alfredsson, Tomas Andersson, Mozhgan Dorkhan, Leif Groop, Tiinamaija Tuomi, Alicja Wolk, Sofia Carlsson

Abstract read
In one paragraph

Article in European journal of nutrition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Insulin Autoimmune Syndrome as Part of Pre-Clinical LADA.Diabetes, metabolic syndrome and obesity : targets and therapy · 2021
    Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Josefin E LöfvenborgInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden. josefin.lofvenborg@ki.se.ORCID http://orcid.org/0000-0002-0099-969X
Emma AhlqvistDepartment of Clinical Sciences, Lund University, Malmö, Sweden.
Lars AlfredssonInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Tomas AnderssonInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Mozhgan DorkhanDepartment of Clinical Sciences, Lund University, Malmö, Sweden.
Leif GroopDepartment of Clinical Sciences, Lund University, Malmö, Sweden.
Tiinamaija TuomiFinnish Institute of Molecular Medicine, Helsinki University, Helsinki, Finland.
Alicja WolkInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Sofia CarlssonInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.

Funding

European Research Council Advanced Researcher Grant GA 269045
6 · The paper itself

Abstract

purposeSweetened beverage consumption is associated with type 2 diabetes (T2D) and LADA. We investigated to what extent this association is mediated by BMI and whether it is modified by genotypes of HLA, TCF7L2 rs7903146, or FTO rs9939609.

methodsSwedish case-control data including incident cases of LADA (n = 386) and T2D (n = 1253) with matched population-based controls (n = 1545) was used. We estimated adjusted ORs of diabetes (95% CI) in relation to sweetened beverage intake (per daily 200 mL serving) and genotypes. The impact of BMI was estimated using causal mediation methodology. Associations with HOMA-IR and HOMA-B were explored through linear regression.

resultsSweetened beverage intake was associated with increased risk of LADA (OR 1.15, 95% CI 1.03-1.29) and T2D (OR 1.21, 1.11-1.32). BMI was estimated to mediate 17% (LADA) and 56% (T2D) of the total risk. LADA was associated with risk variants of HLA (3.44, 2.63-4.50) and TCF7L2 (1.27, 1.00-1.61) but not FTO. Only among non-carriers of high-risk HLA genotypes was sweetened beverage intake associated with risk of LADA (OR 1.32, 1.06-1.56) and HOMA-IR (beta = 0.162, p = 0.0047). T2D was associated with TCF7L2 and FTO but not HLA, and the risk conferred by sweetened beverages appeared modified by FTO (OR 1.45, 95% CI 1.21-1.73 in non-carriers).

conclusionsOur findings suggest that sweetened beverages are associated with LADA and T2D partly through mediation by excess weight, but possibly also through other mechanisms including adverse effects on insulin sensitivity. These effects seem more pronounced in individuals without genetic susceptibility.

Indexed as

Alpha-Ketoglutarate-Dependent Dioxygenase FTOBody Mass IndexCase-Control StudiesDiabetes Mellitus, Type 2FemaleHLA AntigensHumansIncidenceLatent Autoimmune Diabetes in AdultsMaleMiddle AgedSugar-Sweetened BeveragesSwedenTranscription Factor 7-Like 2 ProteinAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanHLA AntigensTCF7L2 protein, humanTranscription Factor 7-Like 2 ProteinAutoimmune diabetesBMIGenotypeLatent autoimmune diabetes in adultsSweetened beverageT2D

Identifiers

PMID30656477
PMCPMC7000500

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.